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rs3934861

From SNPedia

Orientationminus
Stabilizedminus
Make rs3934861(C;C)
Make rs3934861(C;T)
Make rs3934861(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position24105466
GeneMYOM3
is asnp
is mentioned by
dbSNPrs3934861
dbSNP (classic)rs3934861
ClinGenrs3934861
ebirs3934861
HLIrs3934861
Exacrs3934861
Gnomadrs3934861
Varsomers3934861
LitVarrs3934861
Maprs3934861
PheGenIrs3934861
Biobankrs3934861
1000 genomesrs3934861
hgdprs3934861
ensemblrs3934861
geneviewrs3934861
scholarrs3934861
googlers3934861
pharmgkbrs3934861
gwascentralrs3934861
openSNPrs3934861
23andMers3934861
SNPshotrs3934861
SNPdbers3934861
MSV3drs3934861
GWAS Ctlgrs3934861
GMAF0.4986
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23092984OA-icon.png]
Trait Bipolar disorder (mood-incongruent)
Title Genome-wide association of mood-incongruent psychotic bipolar disorder.
Risk Allele
P-val 4E-6
Odds Ratio 1.25 [NR]